Hem/Onc Flashcards

1
Q

How to differentiate between alpha and beta thalassemia

A

Electrophoresis, beta thalassemia will have increased hemoglobin A2

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2
Q

Dx and Management of HIT

A

Dx: clinical, definitive test is serotonin release assay
Stop all heparin products
Transition to argatroban or fondaparinux
Start warfarin when platelet count >150,000 and after treatment with another anticoagulant

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3
Q

Findings on EGD of patient with pernicious anemia

A

Atrophy in the gastric fundus and body (absent rugae)

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4
Q

TTP

A

Due to acquired antibodies against ADAMTS13

Needs plasma exchange to antibodies and replenish ADAMTS13 levels from donor

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5
Q

CML

A

Translocation of chromosomes 9 and 22, creates a bcr-abl fusion protein that leads to unregulated stimulation of the tyrosine kinase system
Tx w/ tyrosine kinase inhibitor

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6
Q

Tx for prolonged bleeding time in patients with renal dysfunction

A

IV desmopressin, works be releasing factor VIII:von Willebrand factor multimers from endothelium

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7
Q

Best treatment for methotrexate induced macrocytic anemia

A

Folinic acid (leucovorin) rather than folic acid

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8
Q

Vitamin K reversal

A

Prothrombin complex concentrate (acts within 10min) and vitamin K (takes 12-24h)

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9
Q

Tx of ITP

A

mild or no bleeding:observe

bleeding: IVIG

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